AI Article Synopsis
- 5''-Iodoneplanocin A was synthesized using D-ribose as the starting material.
- This synthesis involved a series of reactions including addition-iodination-elimination, ring-closing metathesis (RCM), and oxidative rearrangement.
- The compound is being studied for its potential use as antiviral and antitumor agents.
Article Abstract
5''-Iodoneplanocin A was enantiopurely synthesized as potential antiviral and antitumor agents starting from D-ribose using an addition-iodination-elimination reaction, a RCM reaction and an oxidative rearrangement.
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| http://dx.doi.org/10.1093/nass/nrn330 | DOI Listing |
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